Job title: Senior CRA
Industry: Medical Device
Location: Irvine, CA, USA
About the Company: The company is pasted the start up phase and has been in the industry for multiple years. They have created multiple class III medical devices and are growing rapidly.
Job Responsibilities: This CRA will supervisor all study management for the companies global clinical trials. The position works directly with clinical and regulatory professionals internally and externally. Working with CRO's and integrating those efforts with agencies, physicians, and scientists. Project coordination, report writing, and budgets, time lines, safety and proper conduct throughout trials.
Qualifications: Strong multitasking, project management skills, ability to coordinate and manage multiple projects. Must be detail oriented, strong attention to detail and strong communication skills. A Bachelors degree in clinical, scientific, or related field. Advanced degree preferred.
Experience: 4+ years of CRA experience in the Medical Device industry, experience with cardiovascular, vascular, and or class III devices. Someone with Study LEad or Study manager along with EDC systems and IDE experience.
Sthree US is acting as an Employment Business in relation to this vacancy.